Abstract

Inspired by how plants transform carbon dioxide to carbohydrates in photosynthesis, researchers have developed an environmentally friendly reaction that adds the greenhouse gas to organic compounds, including biomass-derived molecules. Last week at the American Chemical Society national meeting in San Diego, they described how they used the carboxylation reaction to synthesize a monomer that could help make a substitute for polyethylene terephthalate (PET), the soda-bottle polymer that is one of the world’s largest-volume plastics. They think the chemistry could open a new route for converting biomass into polymeric materials and fuels. CO2 reacting with carbanions and other nucleophilic carbon centers to form carboxylates isn’t a new concept. But generating nucleophiles generally requires reagents such as highly reducing metals or strong organic bases that are energy-intensive to make and difficult to recycle. “These requirements negate the environmental benefit of using CO2 as a substrate and limit the chemistry to low-volume targets,”

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